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Extension to Reactions with Higher Orders

So far, only pseudo-first-order and instantaneous second-order reactions were discussed. In between there is the range of truly second-order behavior for which the continuity equations for A (Eq. 6.3.a-l) or B (Eq. 6.3.a-2), cannot be solved analytically, only numerically. To obtain an approximate analytical solution. Van Krevelen and Hoftijzer [3] dealt with this situation in a way analogous to that apfdied to pseudo-first-order kinetics, namely by assuming that the concentration of B remains approximately constant close to the interface. They mainly considered very fast reactions encountered in gas absorption so that they could set Cm - 0, that is, the reaction is completed in the film. Their development is in terms of the enhancement factor, F. The approximate equation for is entirely analogous with that obtained for a pseudo-first-order reaction Eq. [Pg.321]

This approximate solution is valid to within 10 percent of the numerical solution. Obviously when Cgi, C, then y = y and the enhancement factor equals that for pseudo-first-order. When this is not the case f is now obtained from an implicit equation. Van Krevelen and Hoftijzer solved Eq. 6.3.e-l and plotted F versus y in the diagram of Fig. 6.3.C-2, given in Sec. 6.3.c connecting the results for pseudo-first-order and instantaneous second-order reactions. [Pg.321]

Porter [7] and also Kishinevskii et al. [8] derived approximate equations for the enhancement factor that were found by Alper [9] to be in excellent agreement with the Van Krevelen and Hoftijzer equation (for Porter s equation when y 2) and which are explicit. Porter s equation is  [Pg.321]

For an irreversible reaction of global order m + n(m with respect to A, n with respect to S), the approach followed by Hikita and Asai [10] was very similar to that of Van Krevelen and Hoftijzer. The rate of reaction was written as  [Pg.322]

Furthermore, Cj was considered to be nearly constant in the film, while was again set zero. Hikita and Asai again cast the results into the form of a physical absorption rate multiplied by an enhancement factor [Pg.322]


See other pages where Extension to Reactions with Higher Orders is mentioned: [Pg.321]    [Pg.322]    [Pg.340]   


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